LOINC long common name : FLT3 gene.p.Asp835 Ile836 mutations [Presence] in Blood or Tissue by Molecular genetics
method;
LOINC short name : FLT3 p.D835 I836 Bld/T Ql;
LOINC description : Point mutations and deletions of codons D835 and I836 within the second tyrosine kinase
domain (protein activation loop) of the FLT3 gene are detected by molecular genetic
methods (e.g. PCR-based assays). This code was created for, but not limited to Invivoscribe's
LeukoStrat(tm) FLT3 Gel Detection Mutation Assay, which detects the presence or absence
of either D835 or I836 mutations within the second TKD but does not identify specific
TKD mutations. FLT3-TKD mutations occur in approximately 7% of patients with acute
myelogenous leukemia (AML).;
Has component